Unique and rewarding experience for a Clinical Research Coordinator who is highly motivated with keen attention to detail to manage study patients in a specialized outpatient-based practice in Greer, SC. This per diem position (2 days a week/16 hours a week, Thursday and Friday highly preferred), in a clinical office setting.
The Clinical Research Coordinator will be responsible for the day-to-day study requirements such as subject recruitment, patient consent, data entry, documentation, and assist where needed.
Essential Duties and Functions
Recruitment and retention of all study participants including tracking
Organization of all patient visits, including screening obtaining consent
Accurate and timely data entry and documentation
Patient correspondence throughout the study
Maintain records for the clinical study and regulatory documents
Some clinical duties including, but not limited to, obtaining vital signs
High School Diploma or above
Strong organization skills with an attention to detail
At least two years of related work experience
Ability to multi-task and work independently
CRC/CCRC Certification/Degree a plus
Medical/Healthcare background a plus
Clinical research/clinical trial experience a plus
LVN's welcome to apply!
CATEGORY: CLINICAL RESEARCH
intraFUSION is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin.
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